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Nitrogenous bases covalently linked to a sugar with and without phosphate groups; used for synthesis, cell signaling, and as cofactors in enzymatic reactions; includes pyrimidine, purine, pyridine, flavin, pyrrolopyrimidine, and triazole varieties.
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Nicotinamide riboside chloride is a nicotinamide (vitamin B3) riboside salt and an NAD+ precursor commonly used in metabolic and aging research to elevate intracellular NAD+ and modulate sirtuin activity. It is supplied as a high-purity solid and as a DMSO solution for use in biochemical and cell-based assays, and is provided with supporting documentation such as a COA and SDS.
Increases intracellular NAD+ levels.
Activates sirtuin enzymes such as SIRT1 and SIRT3.
Available as solid and DMSO solution for assay flexibility.
High purity suitable for biochemical and cell-based studies.
Provided with certificate of analysis and safety data sheet.
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7-deaza-2'-deoxyadenosine is a deoxynucleoside analog used as a biochemical reagent for research applications. It is used in studies of nucleic acid structure and function, and has been reported to inhibit DNA synthesis and related polymerase reactions.
Oligodeoxynucleotide analog for biochemical research.
Reported inhibitor of DNA synthesis and polymerase activity.
Molecular formula: C11H14N4O3.
Molecular weight: 250.25 g/mol.
CAS number: 60129-59-1.
Typical purity reported around 98%, minimum 97%.
Available as a 100 mg quantity.
For research use only; not for diagnostic or therapeutic use.
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Alpha-Adenosine is a purine nucleoside analog known for its broad antitumor activity. It primarily targets indolent lymphoid malignancies by inhibiting DNA synthesis and inducing apoptosis.
Purine nucleoside analog
Exhibits broad antitumor activity
Targets indolent lymphoid malignancies
Inhibits DNA synthesis
Induces apoptosis
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Guanosine-15N5 is an isotopically labeled form of Guanosine, where 15N (nitrogen-15) replaces the natural nitrogen atoms in the molecule. Guanosine is a purine nucleoside, formed by the attachment of guanine to a ribose sugar via a β-N9-glycosidic bond. This compound is primarily intended for research purposes.
15N labeled compound
Purine nucleoside
Formed from guanine and ribose
Possesses anti-HSV activity
Suitable for research applications
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Adenosine dialdehyde is a purine nucleoside analogue that potently inhibits S-adenosylhomocysteine hydrolase (SAHH). It is used as a research reagent in biochemical and cellular studies to probe methylation pathways and methyltransferase activity. The compound is a crystalline solid with molecular weight 265.23 g/mol and formula C10H11N5O4, and it is soluble in DMSO.
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ATP-Red 1 is a multisite-binding switchable fluorescent probe that selectively and rapidly responds to intracellular concentrations of ATP in living cells (Ex/Em = 510/590 nm). It is for research use only.
Selectively and rapidly responds to intracellular ATP in living cells.
Multisite-binding switchable fluorescent probe.
Excitation/Emission at 510/590 nm.
Solid appearance, pale purple to purple color.
Molecular formula: C34H36BN3O4.
Recommended storage: 4°C, protect from light.
In solvent storage: -80°C for 6 months; -20°C for 1 month (protect from light).
Solubility in DMSO: 50 mg/mL (89.05 mM).
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2p-O-Methyl-2-Amino-ATP is a modified nucleoside triphosphate incorporating methylation at the ribose 2 -hydroxyl group and an amino substitution at the 2 position of the adenine base It is designed to alter nucleotide biochemical properties impacting RNA stability and structure upon enzymatic incorporation In in vitro transcription assays 2p-O-Methyl-2-Amino-ATP demonstrates an ability to increase RNA resistance to exonuclease-mediated degradation and induce altered RNA secondary structures Based on these properties 2p-O-Methyl-2-Amino-ATP holds research potential in studies of RNA folding dynamics stability assays RNA-protein interactions and analyses involving chemically modified RNA in biomedical research
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2p-O-Methyl-2-Amino-ATP is a modified nucleoside triphosphate incorporating methylation at the ribose 2 -hydroxyl group and an amino substitution at the 2 position of the adenine base It is designed to alter nucleotide biochemical properties impacting RNA stability and structure upon enzymatic incorporation In in vitro transcription assays 2p-O-Methyl-2-Amino-ATP demonstrates an ability to increase RNA resistance to exonuclease-mediated degradation and induce altered RNA secondary structures Based on these properties 2p-O-Methyl-2-Amino-ATP holds research potential in studies of RNA folding dynamics stability assays RNA-protein interactions and analyses involving chemically modified RNA in biomedical research
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More